Feb. 20, 1952 NOTES 1091 Using SO', S',

Feb. 20, 1952. NOTES. 1091 values of k, and ki are the same for the two forms. Using SO', S', Soa and Sa for the solubilities of the racemic and activ...
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Feb. 20, 1952

NOTES

values of k, and ki are the same for the two forms. Using SO',S', Soaand Sa for the solubilities of the racemic and active forms in water and salt solutions, Eq. (3) can be applied to the results for each. Then, for solubility experiments in solutions of a given salt, k,C, can be eliminated giving

I n practice when the data obey the Setschenow equation it is more convenient to use

1091

high solubility, salt effects obtained from solubility studies can be quite different from those obtained by other procedures, for example vapor pressure or distribution. One of us (W. F. M.) acknowledges with gratitude a Fellowship from the du Pont Grant-in-Aid for Fundamental Research. DEPARTMENT OF CHEMISTRY CORNELL UNIVERSITY ITHACA, NEWYORK RECEIVEDKOVEMBER 14, 1951

Coordination of Silver Ion with Methyl Esters of Oleic and Elaidic Acids Once ki is obtained, the value of k, can be calFulated from Eq. (3)) written for either form. Table I gives the results of such calculations for several salts. In making the calculations the recorded molal concentrations have been converted to molar using an apparent molar volume of 125 ml./mole for mandelic acid. Actually the results are very similar if molal concentrations and activity coefficients are used throughout. Where necessary, notably for experiments with the mandelate salts, corrections for the dissociation of mandelic acid have been made.

BY PETERL. NICHOLS,J R . ~

The coordination of silver ion with unsaturated compounds has been studied extensively by Lucas and co-workers.2*s Their information was obtained largely by partition studies using carbon tetrachloride and 1 N aqueous silver nitrate as the immiscible solvent pair. An attempt to determine the argentation constants of methyl oleate and methyl elaidate with the above solvent pair was quickly found to be impractical since the amount of material transferred to the aqueous silver nitrate phase was negligible. Preliminary experiments TABLE I showed that satisfactory results could be obtained SALTINGOUT AND SELF-INTERACTION PARAMETERS FOR with isooctane as one phase and aqueous methanol MANDELIC ACIDAT 25' as the other phase. The cis-isomer was found to Salt K' Ka ki k. have a greater argentation constant than the trans-isomer, but the magnitudes of the constants LiCl 4-0.40 4-0.20 -0.30 0.125 for the most part were considerably greater than NaCl .30 .185 - .25 .12 those found for cis- and trans-olefins distributed f .I55 f . I O KCl - .22 .07 between carbon tetrachloride and 1 N aqueous RbCl ,135 f .072 - .28 .04 silver nitrate. Accordingly, it is recognized that a CSCl - ,002 - .001 . . , - .002 distribution of this type might be used as a basis NHiCl .21 .I1 - .26 .07 for the separation of cis- and trans-isomers as well LiN03 .21 .115 - .27 .07 as for the separation of saturated and unsaturated NaN Os ,095 .07 ... .04 fatty acid esters or olefinic compounds in general. KNOi - .04 - .OO . . . - .02

+ + +

+ + +

+

CsNOs Na Mandelate CsMandelate

-

,165 .35 .89

-

.097 .205 .31

Av.

-

-

.22 .23 .27

-

.255

-

.06 .12 .18

The most significant point from Table I is that the values of k i calculated from the data for the various salts are constant to within the variation of the experimental data. Furthermore the resulting values of K , are similar to those for the comparable non-electrolytes, benzoic acid5and phthalic acid." Finally the negative value of k i shows, as expected, that mandelic acid is "salted in" by itself. The average value of ki, - 0.25, is quite large but it seems reasonable when compared with the value for phenol for which, from the freezing point data of Jones and Bury,' the ki value is about -0.16. These results for mandelic acid suggest that a comparison of salt effects from solubility measurements for two non-electrolytes of different solubility can be quite misleading unless the self-interaction is corrected for. Similarly for a non-electrolyte of ( 5 ) (a) I. M. Rolthoff and W. Bosch, J . Phys. Chcm., S6, 1685 (1932); (b) E. Larsson, 2. fihysik. Chem., 159, 299 (1931). (6) A. C. D. Rivett and E. I. Rosenblum, Tvans. Favaday SOC.,S, 297 (1914). (7) E. R. Jones and C. R. Bury, Phil. Mag.,17) 4, 1125 (1927).

Experimental Preparation of Materials.-We are indebted to H. B. Knight for generous samples of methyl oleate and methyl elaidate. The iodine values of these preparations were about one unit lower than theoretical. However, the only possible contamination (as indicated by spectrophotometric analysis) was that of saturated esters and these would have a negligible effect on the distribution experiments. Reagent grade chemicals were used throughout. Isooctane (A.S.T.M. grade) had an iodine value of 0.07, a satisfactorily low value. Solutions of isooctane and methanol containing various amounts of water were prepared as follows: upper layer, a large amount of isoktane was shaken successively with several small portions of methanol containing a given amount of water; lower layer, methanol containing a given amount of water was shaken successively with several small portions of isooctane. The solutions of isooctane saturated with a particular methanol solution were added t o weighed amounts of the methyl esters in a volumetric flask and made t o the mark a t 25 =t0.01'. All solutions were stored a t this temperature until used in the distribution experiments. Solutions of aqueous methanol containing silver nitrate were prepared by dissolving silver nitrate in the appropriate amount of water and then diluting t o the mark and saturating the solution as described above. Flasks containing the silver nitrate solutions were wrapped a t all times with a (1) Jet Propulsion Laboratory, California Institute of Technology, Pasadena, California. (2) S. Winatein nnd H. J. Lucas, TRW JOUENAL, 60, 836 (1938). (3) R.J. Lucas, R. S. Moore and D. Pressman, ibid., 65, 227 (1943).

1092

VOl. 74

NOTES

black cloth. Solutions of potassium nitrate were made up in a similar manner. Apparatus and Procedure.-A; distributions were carried Iodine flasks of 250-ml. out in a water-bath at 25 i 0.01 capacity, equipped with mercury seal type stirrers but using glycerol as a seal, were used. A piece of glass tubing sealed to the end of a glass rod effectively stirred the layers, which appeared in the form of a h e emulsion during the stirring. Several runs in which the flasks were flushed with uitrogen before starting the experiment showed no difference from those carried out in air. Twenty ml. of saturated isooctane solution containing approximately 0.3 g. of ester was added to 20 ml. of the aqueous methanol solution saturated with isooctane. Stirring was continued for 30 minutes. Stirring for longer periods gave the same results. Usually the layers separated completely in less than 30 minutes. X 10-ml. sample of upper layer was withdrawn for analysis with the aid of a Luer syringe attached to a pipet by means of rubber tubing. Analytical Procedure.-The customary procedure using Wijs solution4 proved satisfactory for the analysis of the upper layer provided that the sample was allowed to stand one hour in contact with reagent. In each analysis 10 ml. of Wijs solution was added to 10 ml. of the upper layer from a distribution experiment. A blank was run on 10 ml. of isooctane saturated with the appropriate methanol solution.

.

TABLEI ARGENTATIONCONSTANTS AND DISTRIBUTION RATIOFOR THE DISTRIBUTION OF METHYLOLEATEAND METHYL ELAIDATE BETWEEN ISOOCTANE AND AQUEOUS METHANOL' Concn. of methanol,

%

60 90 95

concn. of AgNOs. N

1.0 0.2

Methyl oleated

KD

KO 0.02 .46'

KE

Methyl elaidated KD KP KE

._. .. ... ..

0.02 . . . .17 . . .

.IO 10.5 .79 8 . 2 10.1 .%9 2.9 100 .05 4.2 2.02 8.4 3.9 .81 3 . 1 a Except where noted the average value for two runs is recorded. Too high for a reasonable estimate by the analytical method used. Average value for three runs. Initial concentration in isooctane layer is approx. 0.05 molar.

it bas been shown that relatively large amounts of methyl oleate and methyl elaidate can be removed from isoijctane in a single extraction. The fraction of olefin removed in a single extraction is shown in equation (2) which was checked experimentally.

Results and Discussion The notation and assumptions regarding activities of previous workers2J were used with the substitution of isooctane for carbon tetrachloride and aqueous methanol for water. The argentation constant, KO,has been expressed previously2 by equation (I).

I n order to attain anything like complete separation a number of successive extractions would be required. The technique of countercurrent distribution, as employed by or paper chromatography could be easily adapted to the solvent KO = combinations used in the present work. In a (Bt)sN AgHOi - (B)ino/Ko Craig apparatus the number of transfers, n, re(1) (B)ino[A@)sN&Not - ((Bt1.N &NO, - (B)iso/R~)1 quired to obtain a desired separation can be calIf K D is very large the term (B)iso/KD may be culated by approximate relations derived by neglected in Eq. (1). However, in most of our Nichols.' Using the argentation constants for work this approximation could not be used. methyl oleate and methyl elaidate for 90% methIf one can alter K D without materially altering anol and 0.2 M silver nitrate, calculations show that KE,the effect will be reflected by a corresponding approximately 300 transfers would be required for change in KO. One way to alter K D is to change reasonably complete separation. the ratio of water to methanol in the aqueous Acknowledgment.-I am indebted to G. C. phase. Another way is to change the ionic strength Nutting and B. A. Brice for advice and encourageof the phase containing silver nitrate. ment throughout the course of this investigation. From the above discussion it is apparent that REGIONAL RESEARCH LABORATORYE KE is to be preferred to KO as a measure of the EASTERN 18, PENNSYLVANIA relative coordination tendencies of double bonds in PHILADELPHIA RECEIVED OCTOBER 26, 1951 different types of olefins, but when the substances (5) L. C. Craig, J . B i d . Chcm., 155, 519 (1944). being compared have essentially the same dis(6) L.C. Craig and 0. Post, Anal. Chcm., 21, 500 (1949). tribution constants, as for example cis- and trans(7) P.L. Nichols, Jr., ibid.. 22, 915 (1950). (8) One of the laboratories of the Bureau of Agricultural and Indusisomers, KO would serve as an adequate measure trial Chemistry. Agricultural Research Administration, United States of these tendencies under the same conditions. The constants obtained for the isomeric methyl Department of Agriculture. Article not copyrighted. oleate and methyl elaidate in several solvent combinations are shown in Table I. The striking Benzyl Esters of Amino Acids* differences in argentation constants for the two BY HERBERT K. MILLER* AND HEINRICH WAELSCH isomers are in close agreement, even to order of magnitude, with previous observations. It apThe synthesis of carboxyl-substituted peptides is pears from the limited data in Table I that KE greatly facilitated by the use of benzyl esters of amino is relatively unaffected by changes in methanol acids instead of the commonly employed ethyl esconcentration and that KOis inversely proportional ters since the benzyl group can be removed by hydroto K D but this is not certain. Experimental error genation with palladium catalyst under the same in the measurements, together with possible large conditions as used for the removal of the carbobenzchanges in activity coefficient due to large changes oxy group thus avoiding the need for saponification.s in silver ion concentrations, obscure any accurate (1) This report is in part from a dissertation submitted by Herbert interpretation of the differences in equilibrium K. Miller in partial fulfilment of the requirements for the degree of Doctor of Philosophy in the Faculty of Pure Science, Columbia Uniconstants. By use of increasing concentrations of methanol versity. (2) Atomic Energy Commission Predoctoral Fellow, 1949-1950. (4) A. R. Kemp and G . S. Mueller, I n d . Eng.

(1934).

C h . ,Anal. Ed., 6,52

(3) M. Bergmann, L. Zervas and W.F. Ross, J. Biol. Chcm., 111, 245 (1935).